Primary Device ID | 00670482000142 |
NIH Device Record Key | 86c7ed56-07ff-4cd8-8e4f-c3c4cea66721 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ook snow ALL |
Version Model Number | 200-0000 |
Catalog Number | 200-0000 |
Company DUNS | 249675476 |
Company Name | Umano Medical Inc |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00670482000142 [Primary] |
GS1 | 10670482000149 [Package] Package: [1 Units] In Commercial Distribution |
FNL | Bed, Ac-Powered Adjustable Hospital |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-09-21 |
Device Publish Date | 2018-08-21 |
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